(b)(4).To date, the device has not been returned.If the product is returned for evaluation, any further information derived from the evaluation will be submitted in a supplemental 3500a form.Mwr-16092020-0000805856 submitted for adverse event which occurred on (b)(6) 2008.Mwr-16092020-0000805857 submitted for adverse event which occurred on (b)(6) 2008.Mwr-16092020-0000805858 submitted for adverse event which occurred on (b)(6) 2012.
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It was reported by an attorney that the patient underwent hernia repair surgery on (b)(6) 2007 and mesh was implanted.It was reported that the patient underwent hernia repair surgery on (b)(6) 2008 and mesh was implanted.It was reported that the patient underwent revision surgery on (b)(6) 2008 and on (b)(6) 2012.It was reported that the patient experienced severe and chronic pain, inflammation, adhesions, mesh invading into the dome of the bladder, scarring and mesh separation.Other implanted product is captured in a separate file.No additional information is provided.
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